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审核状态: Project audit state: |
通过审核 Successful |
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注册号: Registration number: |
ChiCTR2000034053 |
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最近更新日期: Date of Last Refreshed on: |
2020-06-22 03:19:54 |
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注册时间: Date of Registration: |
2020-06-21 00:00:00 |
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注册号状态: |
预注册 |
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Registration Status: |
Prospective registration |
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注册题目: |
碳酸氢钠林格氏液应用于围术期单肺通气患者液体治疗的有效性级安全性 |
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Public title: |
the effectiveness and safty of sodium bicarbonate Ringer's solution in perioperative fluid therapy for patients with one lung ventilation |
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注册题目简写: |
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English Acronym: |
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研究课题的正式科学名称: |
碳酸氢钠林格氏液应用于围术期单肺通气患者液体治疗的有效性级安全性 |
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Scientific title: |
the effectiveness and safty of sodium bicarbonate Ringer's solution in perioperative fluid therapy for patients with one lung ventilation |
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研究课题代号(代码): Study subject ID: |
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在二级注册机构或其它机构的注册号: The registration number of the Partner Registry or other register: |
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申请注册联系人: |
宋洁 |
研究负责人: |
张野 |
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Applicant: |
Song Jie |
Study leader: |
Zhang Ye |
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申请注册联系人电话: Applicant telephone: |
+86 13500504205 |
研究负责人电话:
Study leader's |
+86 13966768081 |
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申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
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申请注册联系人电子邮件: Applicant E-mail: |
1601905832@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
zhangye_hassan@sina.com |
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申请单位网址(自愿提供): Applicant website(voluntary supply): |
研究负责人网址(自愿提供): Study leader's website(voluntary supply): |
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申请注册联系人通讯地址: |
安徽省合肥市芙蓉路678号 |
研究负责人通讯地址: |
安徽省合肥市芙蓉路678号 |
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Applicant address: |
678 Furong Road, Hefei, Anhui, China |
Study leader's address: |
678 Furong Road, Hefei, Anhui, China |
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申请注册联系人邮政编码: Applicant postcode: |
研究负责人邮政编码: Study leader's postcode: |
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申请人所在单位: |
安徽医科大学第二附属医院 |
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Applicant's institution: |
the Second Affiliated Hospital of Anhui Medical University |
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研究负责人所在单位: |
安徽医科大学第二附属 |
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Affiliation of the Leader: |
the Second Affiliated Hospital of Anhui Medical University |
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是否获伦理委员会批准: |
是 |
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Approved by ethic committee: |
Yes |
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伦理委员会批件文号: Approved No. of ethic committee: |
YX2020-002(F1) |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
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批准本研究的伦理委员会名称: |
安徽医科大学第二附属医学研究伦理委员会 |
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Name of the ethic committee: |
the Second Hospital of Anhui Medical University, Ethics Commitee |
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伦理委员会批准日期: Date of approved by ethic committee: |
2020-06-03 00:00:00 | ||
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伦理委员会联系人: |
张静 |
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Contact Name of the ethic committee: |
Zhang Jing |
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伦理委员会联系地址: |
安徽省合肥市芙蓉路678号 |
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Contact Address of the ethic committee: |
678 Furong Road, Hefei, Anhui, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
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研究实施负责(组长)单位: |
安徽医科大学第二附属医院 |
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Primary sponsor: |
the Second Affiliated Hospital of Anhui Medical University |
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研究实施负责(组长)单位地址: |
安徽省合肥市芙蓉路678号 |
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Primary sponsor's address: |
678 Furong Road, Hefei, Anhui, China |
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试验主办单位(项目批准或申办者): Secondary sponsor: |
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经费或物资来源: |
自筹经费 |
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Source(s) of funding: |
Self- raised |
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研究疾病: |
呼吸和胸腔内气管,其他的恶性肿瘤个人史 |
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Target disease: |
Resipiratory and intrathoracic organs, personal history of other malignant tumors |
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研究疾病代码: |
Z85.200 |
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Target disease code: |
Z85.200 |
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研究类型: |
干预性研究 |
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Study type: |
Interventional study |
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研究所处阶段: |
IV期临床试验 | ||||||||||||||||||||||
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Study phase: |
4 |
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研究设计: |
随机平行对照 |
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Study design: |
Parallel |
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研究目的: |
本研究拟通过前瞻性临床对照试验,在胸腔镜单肺通气患者术中分别应用碳酸氢钠林格氏液和乳酸林格氏液,观察对二氧化碳的释放和酸碱平衡的影响,旨在探讨碳酸氢钠林格氏液在单肺通气患者中应用的有效性和安全性。 |
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Objectives of Study: |
This study intends to use prospective clinical controlled trials to apply sodium bicarbonate Ringer's solution and lactated Ringer's solution in patients undergoing thoracoscope single lung ventilation surgery to observe the effects on carbon dioxide release and acid-base balance. The effectiveness and safety of sodium bicarbonate Ringer's solution in patients with one lung ventilation. |
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药物成份或治疗方案详述: |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
1.择期行胸腔镜手术,术中预计实施单肺通气时间>1h且<4h的患者 |
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Inclusion criteria |
1. Patients undergoing elective thoracoscopic surgery, during which patients are expected to have one lung ventilation time >1h and <4h |
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排除标准: |
1、人工气胸或开胸手术的胸科手术; |
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Exclusion criteria: |
1. Chest surgery for artificial pneumothorax or thoracotomy; |
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研究实施时间: Study execute time: |
从 From 2019-12-30 00:00:00至 To 2023-12-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2020-07-01 00:00:00 至 To 2021-07-07 00:00:00 |
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干预措施: Interventions: |
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研究实施地点: Countries of recruitment and research settings: |
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测量指标: Outcomes: |
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采集人体标本:
Collecting sample(s)
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征募研究对象情况: Recruiting status: |
尚未开始 Not yet recruiting |
年龄范围: Participant age: |
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性别: |
男女均可 |
Gender: |
Both |
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随机方法(请说明由何人用什么方法产生随机序列): |
由第三方统计员管理的计算机化随机数生成器 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
computerised random number generator managed by a third-party statistician |
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是否公开试验完成后的统计结果: Calculated Results after the Study Completed public access: |
公开/Public |
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盲法: |
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Blinding: |
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试验完成后的统计结果(上传文件): |
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Calculated Results after
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是否共享原始数据: IPD sharing |
否No |
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共享原始数据的方式(说明:请填入公开原始数据日期和方式,如采用网络平台,需填该网络平台名称和网址): |
ResMan平台 www.medresman.org.cn |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
ResMan www.medresman.org.cn |
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数据采集和管理(说明:数据采集和管理由两部分组成,一为病例记录表(Case Record Form, CRF),二为电子采集和管理系统(Electronic Data Capture, EDC),如ResMan即为一种基于互联网的EDC: |
1.数据的采集:本试验采用专人对入组患者资料进行收集并根据专用表格填写研究记录,用于记录受试者第一手临床试验数据资料。 2.数据的报告:CRF为统计源文件,由研究者填写。由申办者或其指定人员提供病例报告表(CRF),应按照提供的说明处理CRF。应由授权的研究人员完整填写所有CRF。完成的CRF,第一联交统计分析单位,进行数据录入工作。第一联移交后,CRF的内容不再作修改。 3.数据的监查:监查员的人数与访视频度必须满足临床试验的质控要求。 4.数据的录入及核查 (1)建立数据库:由数据管理与统计分析单位负责。 (2)核查数据:数值范围和逻辑检查,如有疑问通过监查员向研究者发出询问,研究者应尽快解答并返回,数据管理员根据研究者的回答进行数据修改,确认与录入。 5.数据可溯源性的规定:应保存质量控制性文件,如数据一致性检查,数值范围和逻辑检查的原始记录,盲态核查时的原始记录、研究者与监查员之间交流的疑问记录等。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
1. Data collection: In this trial, a special person is used to collect the data of the enrolled patients and fill in the research records according to the special form, which is used to record the first-hand clinical trial data of the subjects. 2. Data report: CRF is a statistical source file, filled in by the researcher. The case report form (CRF) is provided by the sponsor or its designated personnel, and the CRF should be processed according to the instructions provided. Authorized researchers should complete all CRFs. The first couplet of the completed CRF will be performed to statistical analysis unit. After the transfer of the first couplet, the contents of the CRF will not be modified. 3. Data monitoring: The number of inspectors and the interview frequency must meet the quality control requirements of clinical trials. 4. Data entry and verification (1) Establish a database: the data management and statistical analysis unit is responsible. (2) Check the data: the value range and logic check. If there is any doubt, the investigator should send an inquiry to the investigator. The investigator should answer and return as soon as possible. The data administrator will modify the data according to the investigator's answer, confirm and enter it. 5. Provisions for data traceability: Preserving the quality control documents, such as the original records of data consistency checks, numerical ranges and logical checks, the original records of blind inspections, and communication questions between researchers and supervisors Records. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |